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Clinical Trials in China / NCT06105970
Recruiting Observational

Chinese Community Sample of Hierarchical Model of Psychopathology

NCT06105970 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai Mental Health Center
Phase
Observational
Started
2023-09-26
Last updated
2025-07-10

Condition(s) studied

Mental Health IssueAdverse Childhood Experience

Investigational drug(s) / intervention(s)

No intervention

No intervention: cross sectional study#no intervention

Study summary

By validating Hierarchy Model of psychopathology(HiTOP) in Chinese community samples, this study aims for illumating the problem of diagnostic heterogeneity and high comorbidity within existing psychiatric classification systems in Chinese culture. Concurrently, this study also focuses on exploring trans-diagonostic risk and proctective factors underline HiTOP dimensions.

the main questions it aims to answer are:

1. Explore HiTOP model cultural differences between western culture and eastern culture.
2. Understand the impact of different dimension of adverse childhood experience on HiTOP structure.
3. Investigate the relationship between individual unique psychological variables and psychopathological dimensions.

Participants will receive a detailed survey trying to measure their psychopathology symptoms, adverse childhood experience and psychological variables. This study expects to fallow up participants for 4 years to monitor the symptom changes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
Accepted
Inclusion Criteria: 1. Chinese citizens 2. Years of education \> =9 years. 3. age \>= 18 years old. Exclusion Criteria: (1)Subjects who have insufficient self-awareness, and are unable to obtain complete informed consent, such as: schizophrenia, manic episode of bipolar disorder, severe depression.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shanghai Mental Health Center Shanghai China Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06105970 on ClinicalTrials.gov ↗ ← All trials in China